Association of vitamin D deficiency with hepatitis B virus - related liver diseases.

Association of vitamin D deficiency with hepatitis B virus - related liver diseases.
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维生素D缺乏与乙型肝炎病毒相关肝病的关系。

DOI:
10.1186/s12879-016-1836-0
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发表时间:
2016-09-23
影响因子:
3.7
通讯作者:
Song LH
Song LH
中科院分区:
医学3区
文献类型:
--
作者:
Hoan NX;Khuyen N;Binh MT;Giang DP;Van Tong H;Hoan PQ;Trung NT;Anh DT;Toan NL;Meyer CG;Kremsner PG;Velavan TP;Song LH

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作为免疫调节剂,维生素D参与多种疾病的各种病理生理机制。本研究旨在将越南患者中与B型肝炎病毒(HBV)感染相关的肝脏疾病的维生素D缺乏状态与临床进展相关联,并将其与健康对照组进行比较。我们定量了400例HBV患者(慢性乙型肝炎B感染[CH B],n = 165; HBV相关肝硬化[LC],n = 127; HBV相关肝细胞癌[HCC],n = 108)和122例无关健康对照(HC)血清样本中总维生素D [25-(OH)D2和D3]的水平。进行单变量和多变量分析,以确定维生素D水平和不同的临床参数之间的关联。维生素D不足(<30 ng/mL)的患病率在健康个体(81.7%)和HBV患者(84.3%)中较高。维生素D缺乏(<20 ng/ml)或严重缺乏(<10 ng/ml)在HBV患者(52%)和亚组(CHB,47.8%; LC,54.4%; HCC,55.3%)中比对照组(32.5%)更常见(P < 0.001)。维生素D水平和HBV-DNA载量呈强负相关(rho =-0.57,P < 0.0001)。多元回归分析也显示HBV-DNA载量与低维生素D水平独立相关(P = 0.0004)。此外,维生素D水平降低与LC的显著临床进展相关(Child-Pugh C与Child-Pugh A,P = 0.0018; Child-Pugh C与Child-Pugh B,P = 0.016)。在大多数HBV感染患者中观察到维生素D缺乏,并与不良临床结局相关。我们的研究结果表明,维生素D替代可能是治疗慢性肝病,特别是HBV相关疾病的支持性选择。
As an immune modulator, vitamin D is involved in various pathophysiological mechanisms in a plethora of diseases. This study aims to correlate the vitamin D deficiency status and clinical progression of liver diseases associated with hepatitis B virus (HBV) infection in patients in Vietnam and to compare it to healthy controls. We quantified the levels of total vitamin D [25-(OH) D2 and D3] in serum samples from 400 HBV patients (chronic hepatitis B infection [CHB], n = 165; HBV-associated liver cirrhosis [LC], n = 127; HBV-associated hepatocellular carcinoma [HCC], n = 108) and 122 unrelated healthy controls (HC). Univariate and multivariate analyses were performed in order to determine the association between vitamin D levels and distinct clinical parameters. The prevalence of vitamin D inadequacy (<30 ng/mL) was high among healthy individuals (81.7 %) as well as in HBV patients (84.3 %). Vitamin D deficiency (<20 ng/ml) or severe deficiency (<10 ng/ml) was observed more frequently among HBV patients (52 %) and subgroups (CHB, 47.8 %; LC, 54.4 %; HCC, 55.3 %) compared to the control group (32.5 %) (P < 0.001). Vitamin D levels and HBV-DNA load were strongly and inversely correlated (rho = −0.57, P < 0.0001). Multivariate regression analysis also revealed an independent association of HBV-DNA loads with low vitamin D levels (P = 0.0004). In addition, reduced vitamin D levels were associated with significant clinical progression of LC (Child-Pugh C versus Child-Pugh A, P = 0.0018; Child-Pugh C versus Child-Pugh B, P = 0.016). Vitamin D deficiency was observed in the majority of HBV-infected patients and associated with adverse clinical outcomes. Our findings suggest that substitution of vitamin D may be a supportive option in the treatment of chronic liver diseases, in particular of HBV-associated disorders.
DOI: 10.1371/journal.pone.0064053
发表时间: 2013
期刊: PloS one
影响因子: 3.7
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发表时间: 1994-10-01
影响因子: 7.1
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DOI: 10.1007/s10557-015-6629-y
发表时间: 2015-12-01
影响因子: 3.4
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DOI: 10.1210/jc.2004-2364
发表时间: 2005-06-01
影响因子: 5.8
作者:
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通讯作者: de Papp, AE